(Q53064258)

11 May 2018

meta-analysis

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title

Complement factor H Y402H gene polymorphism and coronary heart disease susceptibility: a meta-analysis. (English)

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11 May 2018

main subject

coronary artery disease

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Hai-Feng Zhang

1

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11 May 2018

Jing-Feng Wang

2

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11 May 2018

Yan Wang

3

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11 May 2018

Li-Guang Zhu

4

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11 May 2018

Lei Lei

5

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11 May 2018

publication date

3 February 2010

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11 May 2018

Molecular Biology Reports

published in

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11 May 2018

volume

38

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11 May 2018

issue

5

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11 May 2018

page(s)

2933-2938

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11 May 2018

https://scigraph.springernature.com/pub.10.1007/s11033-010-9956-x

exact match

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CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration

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Critical appraisal of CRP measurement for the prediction of coronary heart disease events: new data and systematic review of 31 prospective cohorts

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21 January 2018

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A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study

21 January 2018

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Complement factor H Y402H gene polymorphism, C-reactive protein, and risk of incident myocardial infarction, ischaemic stroke, and venous thromboembolism: a nested case-control study

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21 January 2018

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21 January 2018

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The common Y402H variant in complement factor H gene is not associated with susceptibility to myocardial infarction and its related risk factors

21 January 2018

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Complement factor H Y402H decreases cardiovascular disease risk in patients with familial hypercholesterolaemia

21 January 2018

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Complement factor H Y402H gene polymorphism in coronary artery disease and atherosclerosis

21 January 2018

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12 December 2020

Lack of association between complement factor H polymorphisms and coronary artery disease or myocardial infarction

1 reference

12 December 2020

Complement factor H Y402H polymorphism, plasma concentration and risk of coronary artery disease

1 reference

12 December 2020

Confounding and misclassification.

1 reference

12 December 2020

1 reference

12 December 2020

10.1007/S11033-010-9956-X

Identifiers

DOI

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11 May 2018

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11 May 2018